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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647142Erstellt: 25. Oktober 2026

Phenacyl bromide → 2-(3,5-Dichlorophenyl)oxirane

https://huagongshe.com/reaction/647142

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenacyl bromideHCID 6259—
EduktStyrene OxideHCID 7276—
EduktEthyl AcetateHCID 8857—
Edukt3',5'-DichloroacetophenoneHCID 2758058—
LösungsmittelChloroformHCID 6212—
Produkt2-(3,5-Dichlorophenyl)oxiraneHCID 13488795—

Reaktionsschritte

The phenacyl bromide intermediate for the above-mentioned styrene oxide is prepared by brominating 10 g of 3,5-dichloroacetophenone in 50 ml of CHCl3 /50 ml of EtOAc with 23.6 g of CuBr2. The mixture is heated at reflux for 2.5 hours and cooled to room temperature. After stirring for 16 hours at room temperature, the mixture is cooled in ice for 2 hours and filtered. The filter cake is washed with 50 ml of CHCl3 and the combined filtrates are twice decolorized with activated carbon, filtered, and evaporated to dryness in vacuo to afford the orange oil of the 3,5-dichlorostyrene oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04407819
Quelldatensatzuspto-grants-1983_10
ORD IDord-acc0afc7627a4a26ab50c75c81da3f4d
Quellennotizuspto-grants-1983_10